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NDC 11673-0089-40 Target Up and Up Kids Mineral Sunscreen SPF 50 45; 65 mg/mL; mg/mL Details

Target Up and Up Kids Mineral Sunscreen SPF 50 45; 65 mg/mL; mg/mL

Target Up and Up Kids Mineral Sunscreen SPF 50 is a TOPICAL LOTION in the HUMAN OTC DRUG category. It is labeled and distributed by TARGET CORPORATION. The primary component is TITANIUM DIOXIDE; ZINC OXIDE.

Product Information

NDC	11673-0089
Product ID	11673-089_baef8c1e-a57a-2042-e053-2a95a90aa08b
Associated GPIs
GCN Sequence Number	n/a
GCN Sequence Number Description	n/a
HIC3	n/a
HIC3 Description	n/a
GCN	n/a
HICL Sequence Number	n/a
HICL Sequence Number Description	n/a
Brand/Generic	n/a
Proprietary Name	Target Up and Up Kids Mineral Sunscreen SPF 50
Proprietary Name Suffix	n/a
Non-Proprietary Name	Titanium Dioxide, Zinc Oxide
Product Type	HUMAN OTC DRUG
Dosage Form	LOTION
Route	TOPICAL
Active Ingredient Strength	45; 65
Active Ingredient Units	mg/mL; mg/mL
Substance Name	TITANIUM DIOXIDE; ZINC OXIDE
Labeler Name	TARGET CORPORATION
Pharmaceutical Class	n/a
DEA Schedule	n/a
Marketing Category	OTC MONOGRAPH NOT FINAL
Application Number	part352
Listing Certified Through	2024-12-31

Package

Package Images

NDC 11673-0089-40 (11673008940)

Pricing Information	N/A
NDC Package Code	11673-089-40
Billing NDC	11673008940
Package	308 mL in 1 BOTTLE (11673-089-40)
Marketing Start Date	2014-01-17
NDC Exclude Flag	N

Standard Product Labeling (SPL)/Prescribing Information SPL baef71c6-d4a6-cc47-e053-2a95a90ad566 Details

Active Ingredients

Titanium Dioxide 4.5%, Zinc Oxide 6.5%

Purpose

Sunscreen

Uses

• helps prevent sunburn • if used as directed with other sun protection measures (see Directions), decreases the risk of skin cancer and early skin aging caused by the sun

Warnings

For external use only

Do not use

on damaged or broken skin.

When using this product

keep out of eyes. Rinse with water to remove.

Stop use and ask doctor if

rash occurs.

Keep out of reach of children.

If product is swallowed, get medical help or contact a Poison Control Center right away.

Directions

apply liberally 15 minutes before sun exposure
reapply:

- after 80 minutes of swimming or sweating

- immediately after towel drying

- at least every 2 hours

Children under 6 months: ask a doctor

Sun Protection Measures. Spending time in the sun increases your risk of skin cancer and early skin aging. To decrease this risk, regularly use a sunscreen with a broad spectrum SPF of 15 or higher and other sun protection measures including:

- limit time in the sun, especially from 10 a.m. - 2 p.m.

- wear long sleeve shirts, pants, hats, and sunglasses

Other infomation

protect this product from excessive heat and direct sun
may stain or damage some fabrics, materials or surfaces

Inactive Ingredients

water, caprylic/capric triglyceride, isohexadecane, butyloctyl salicylate, octyldodecyl citrate crosspolymer, cetyl PEG/PPG-10/1 dimethicone, lauryl PEG-8 dimethicone, C30-38 olefin/isopropyl maleate/MA copolymer, sodium chloride, ethylhexyl methoxycrylene, dimethicone, caprylyl glycol, PEG-8, silica, triethoxycaprylylsilane, glycerin, sodium citrate, tocopheryl acetate, benzyl alcohol, benzoic acid, sorbic acid.

Label

Target Up & Up Kids' Mineral Sunscreen SPF 50 Lotion

10.4 fl oz (307.5 mL)

NDC 11673-089-40

INGREDIENTS AND APPEARANCE

TARGET UP AND UP KIDS MINERAL SUNSCREEN SPF 50

titanium dioxide, zinc oxide lotion

Product Information
Product Type	HUMAN OTC DRUG	Item Code (Source)	NDC:11673-089
Route of Administration	TOPICAL

Ingredient Name	Basis of Strength	Strength
Active Ingredient/Active Moiety
ZINC OXIDE (UNII: SOI2LOH54Z) (ZINC OXIDE - UNII:SOI2LOH54Z)	ZINC OXIDE	65 mg in 1 mL
TITANIUM DIOXIDE (UNII: 15FIX9V2JP) (TITANIUM DIOXIDE - UNII:15FIX9V2JP)	TITANIUM DIOXIDE	45 mg in 1 mL

Ingredient Name	Strength
Inactive Ingredients
OCTYLDODECYL CITRATE CROSSPOLYMER (UNII: X323T6QO4M)
ETHYLHEXYL METHOXYCRYLENE (UNII: S3KFG6Q5X8)
SILICON DIOXIDE (UNII: ETJ7Z6XBU4)
MEDIUM-CHAIN TRIGLYCERIDES (UNII: C9H2L21V7U)
SORBIC ACID (UNII: X045WJ989B)
WATER (UNII: 059QF0KO0R)
CETYL PEG/PPG-10/1 DIMETHICONE (HLB 5) (UNII: 035JKJ76MT)
SODIUM CHLORIDE (UNII: 451W47IQ8X)
GLYCERIN (UNII: PDC6A3C0OX)
ALPHA-TOCOPHEROL ACETATE (UNII: 9E8X80D2L0)
TRIETHOXYCAPRYLYLSILANE (UNII: LDC331P08E)
BENZYL ALCOHOL (UNII: LKG8494WBH)
1,5-PENTANEDIOL (UNII: 07UXZ0SCST)
SODIUM CITRATE (UNII: 1Q73Q2JULR)
BENZOIC ACID (UNII: 8SKN0B0MIM)
CAPRYLYL GLYCOL (UNII: 00YIU5438U)
ISOHEXADECANE (UNII: 918X1OUF1E)
BUTYLOCTYL SALICYLATE (UNII: 2EH13UN8D3)
DIMETHICONE (UNII: 92RU3N3Y1O)
LAURYL PEG/PPG-18/18 METHICONE (UNII: ZJ5S27D9NX)
POLYETHYLENE GLYCOL 4000 (UNII: 4R4HFI6D95)

#	Item Code	Package Description	Marketing Start Date	Marketing End Date
Packaging
1	NDC:11673-089-40	308 mL in 1 BOTTLE; Type 0: Not a Combination Product	01/17/2014

Marketing Category	Application Number or Monograph Citation	Marketing Start Date	Marketing End Date
Marketing Information
OTC monograph not final	part352	01/17/2014

Labeler - TARGET CORPORATION (006961700)

Revised: 2/2021

Document Id: baef8c1e-a57a-2042-e053-2a95a90aa08b

Set id: baef71c6-d4a6-cc47-e053-2a95a90ad566

Version: 1

Effective Time: 20210209